Seguimos Avanzando - Latino Youth Coping With Discrimination

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04875208
Collaborator
University of Notre Dame (Other), Fordham University (Other), Indiana University (Other)
1,020
1
35.7
28.6

Study Details

Study Description

Brief Summary

The overall objective of this study is to investigate mediators and moderators at multiple ecological (individual, family/peer and school/neighborhood levels) and time-scale (micro- and macro-time) levels in the link between discrimination-related stressors and mental health among 340 Mexican-origin youth.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The project's long-term goal is to improve the mental health of Mexican-origin youth by reducing the deleterious effects of racism, "othering," and negative neighborhood interactions. Community based collaboration will be used to recruit a sample of 340 Mexican-origin adolescents, mothers, and fathers in Indiana. The inclusion of fathers will be a valuable contribution to the literature, given the dearth of studies on Latinx fathers/stepfathers. A combination of annual surveys administered over three waves to parents and youth ("macro-time") and a 21-day daily diary ("micro-time") administered in wave 1 to youth is employed to assess important questions about how mediating and moderating processes unfold over time. Specific aims of the project include determination of within-person discrimination-related stressors that impact youth's mental health outcomes and the mechanisms of action at both micro- and macro- time levels; identification of protective factors that could help coping with discrimination related stressors and conditions under which they work; and elucidating youth, parent, and neighborhood risk factors that moderate the link between discrimination-related stressors and mental health outcomes in youth. This research is highly translational in that it will facilitate the development of more effective, culturally sensitive prevention and intervention strategies for Latinx youth and their families.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    1020 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Latino Youth Coping With Discrimination: A Multi-Level Investigation in Micro- and Macro-Time
    Actual Study Start Date :
    Apr 9, 2021
    Anticipated Primary Completion Date :
    Mar 31, 2024
    Anticipated Study Completion Date :
    Mar 31, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Children's Depression Inventory 2nd Edition™: Self-Report Short Form [(CDI-2: SR(S)] [Time 0 (baseline)]

      Youth Depression, Total score 0-24, Higher scores are worse

    2. Children's Depression Inventory 2nd Edition™: Self-Report Short Form [(CDI-2: SR(S)] [Month 12]

      Youth Depression, Total score 0-24, Higher scores are worse

    3. Children's Depression Inventory 2nd Edition™: Self-Report Short Form [(CDI-2: SR(S)] [Month 24]

      Youth Depression, Total score 0-24, Higher scores are worse

    4. Screen for Child Anxiety Related Disorders/ [General Anxiety subscale only] (SCARED) [Time 0 (baseline)]

      Youth Anxiety, Subscale Total score 0-18, Higher scores are worse

    5. Screen for Child Anxiety Related Disorders/ [General Anxiety subscale only] (SCARED) [Month 12]

      Youth Anxiety, Subscale Total score 0-18, Higher scores are worse

    6. Screen for Child Anxiety Related Disorders/ [General Anxiety subscale only] (SCARED) [Month 24]

      Youth Anxiety, Subscale Total score 0-18, Higher scores are worse

    7. Youth Self-Report for Ages 11-18 (YSR/11-18) [Time 0 (baseline)]

      Youth Psychological Symptoms

    8. Youth Self-Report for Ages 11-18 (YSR/11-18) [Month 12]

      Youth Psychological Symptoms

    9. Youth Self-Report for Ages 11-18 (YSR/11-18) [Month 24]

      Youth Psychological Symptoms

    10. Child Behavior Checklist for Ages 6-18 (CBCL/6-18) [Time 0 (baseline)]

      Adaptive Functioning

    11. Child Behavior Checklist for Ages 6-18 (CBCL/6-18) [Month 12]

      Adaptive Functioning

    12. Child Behavior Checklist for Ages 6-18 (CBCL/6-18) [Month 24]

      Adaptive Functioning

    13. Pittsburgh Sleep Quality Index (PSQI) [Time 0 (baseline)]

      Sleep Duration and Quality; Total global score (for unadapted scale) 0-21

    14. Pittsburgh Sleep Quality Index (PSQI) [Month 12]

      Sleep Duration and Quality; Total global score (for unadapted scale) 0-21

    15. Pittsburgh Sleep Quality Index (PSQI) [Month 24]

      Sleep Duration and Quality; Total global score (for unadapted scale) 0-21

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    Adolescent Inclusion Criteria:
    • The adolescent has two eligible caregivers (as defined in the following criteria)

    • The adolescent resides with at least one of the two caregivers.

    • One of the caregivers is a parent or legal guardian who is eligible to give consent for the child's participation.

    Caregiver Inclusion Criteria:
    • Biological Parents of Mexican origin

    • Legal guardians of Mexican origin

    • Step-parents of Mexican origin

    • A caregiver of Mexican origin identified by the parent/guardian who is 18 or older (e.g., grandparents, uncles/aunts, older siblings, godparents)

    Exclusion Criteria:
    • A parent reports that the adolescent has a severe learning or developmental disability which would prevent understanding/survey response

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Notre Dame, William J. Shaw Center for Children and Families South Bend Indiana United States 46635

    Sponsors and Collaborators

    • Massachusetts General Hospital
    • University of Notre Dame
    • Fordham University
    • Indiana University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Margarita Alegria, PhD, Chief, Disparities Research Unit, Massachusetts General Hospital
    ClinicalTrials.gov Identifier:
    NCT04875208
    Other Study ID Numbers:
    • 2020P001721
    First Posted:
    May 6, 2021
    Last Update Posted:
    Dec 21, 2021
    Last Verified:
    Dec 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Dec 21, 2021